Biochemistry tests in Dubai & UAE

Compare available Biochemistry tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

1,113

Listed price range

450.00–30,000.00 AED

Clinical preparation

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Biochemistry test prices

Showing 841–855 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2974 PTH1R Gene Chondrodysplasia, Blomstrand Type Genetic Test This test evaluates the PTH1R gene for pathogenic variants associated with Blomstrand chondrodysplasia.	Peripheral blood (EDTA tube) or extracted genomic DNA	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PTH1R gene", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Novel splice-site mutations"] Parameters [] Preparation [] Indications ["Individuals with clinical or radiological suspicion of skeletal dysplasia", "Individuals with a strong family history of lethal neonatal bone disorders", "Couples with a previous pregnancy affected by Blomstrand chondrodysplasia"] Measurement technique Confirm with laboratory Codes LOINC: 47619-6 ICD-10: Q77.8 Clinical summary This test evaluates the PTH1R gene for pathogenic variants associated with Blomstrand chondrodysplasia.
TEST-2980 PTHrP (Parathyroid Hormone-Related Protein) Test This diagnostic test quantifies parathyroid hormone-related protein (PTHrP) levels in the blood.	Sodium heparin plasma, separated and frozen	2–3 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Parathyroid Hormone-Related Protein (PTHrP) levels"] Parameters [{"name": "PTHrP", "reference_range": null}] Preparation ["No fasting required", "Mandatory signed Test Send Out Consent Form (Form 35)"] Indications ["Diagnosis of humoral hypercalcemia of malignancy (HHM)", "Differentiation of hypercalcemia causes"] Measurement technique Confirm with laboratory Codes LOINC: 3186-6 ICD-10: E83.52 Clinical summary This diagnostic test quantifies parathyroid hormone-related protein (PTHrP) levels in the blood.
TEST-3600 PXDN Gene Corneal Opacification and Other Ocular Anomalies Genetic Test This genetic test analyzes the PXDN gene to detect pathogenic variants causing congenital corneal opacification and associated ocular anomalies.	Whole blood, extracted DNA, cheek swab (buccal mucosa), dried blood spots on FTA cards, ocular fluid	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PXDN gene variants", "Pathogenic mutations"] Parameters [] Preparation ["Mandatory genetic counselling session before sample collection"] Indications ["Clinical suspicion of PXDN-related disease", "Family history of corneal opacification", "Need for recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 94221-7 ICD-10: H17.8 Clinical summary This genetic test analyzes the PXDN gene to detect pathogenic variants causing congenital corneal opacification and associated ocular anomalies.
TEST-6334 PYGL Gene Glycogen Storage Disease Type VI (Hers Disease) Genetic Test This test identifies pathogenic variants in the PYGL gene, confirming a diagnosis of Glycogen Storage Disease Type VI (Hers disease).	Whole blood (3–5 mL), extracted DNA, or FTA card blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PYGL gene mutations", "Pathogenic variants (missense, nonsense, frameshift, splice-site)"] Parameters [] Preparation ["No specific fasting required for blood draw.", "Inform phlebotomist of any medications."] Indications ["Suspected Glycogen Storage Disease Type VI (Hers disease)", "Clinical signs and biochemical testing suggestive of GSD VI"] Measurement technique Confirm with laboratory Codes LOINC: 91818-9 ICD-10: E74.03 Clinical summary This test identifies pathogenic variants in the PYGL gene, confirming a diagnosis of Glycogen Storage Disease Type VI (Hers disease).
TEST-2983 Pyruvate (Pyruvic Acid) Blood Test This diagnostic test evaluates the level of pyruvate, a key intermediate in energy metabolism, in the blood.	Peripheral venous blood (plasma)	Same-day reporting (sample received by 2 pm)	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pyruvate (Pyruvic Acid)", "Glycolysis end product", "Mitochondrial energy metabolism"] Parameters [{"name": "Pyruvate", "reference_range": null}] Preparation ["Fasting is not mandatory, but a 4-hour fast is recommended for best accuracy.", "Inform the laboratory and doctor about all medications and supplements (e.g., metformin, valproic acid)."] Indications ["Assessment of mitochondrial energy metabolism", "Diagnosis of lactic acidosis", "Investigation of inborn errors of metabolism", "Pediatric evaluations", "Neonatal screening", "Sports medicine evaluations"] Measurement technique Confirm with laboratory Codes LOINC: 2648-6 ICD-10: E74.8 Clinical summary This diagnostic test evaluates the level of pyruvate, a key intermediate in energy metabolism, in the blood.
TEST-1177 Quadruple Marker Test This test evaluates maternal serum levels of four specific markers to assess the risk of fetal chromosomal abnormalities and neural tube defects.	Maternal Serum	3–4 Days	600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Alpha-fetoprotein (AFP)", "Human chorionic gonadotropin (hCG)", "Unconjugated estriol (uE3)", "Inhibin A"] Parameters [{"name": "Alpha-fetoprotein (AFP)", "reference_range": null}, {"name": "Human chorionic gonadotropin (hCG)", "reference_range": null}, {"name": "Unconjugated estriol (uE3)", "reference_range": null}, {"name": "Inhibin A", "reference_range": null}] Preparation [] Indications ["Second-trimester prenatal screening for chromosomal abnormalities (Trisomy 21, Trisomy 18)", "Screening for neural tube defects"] Measurement technique Confirm with laboratory Codes LOINC: 49586-2 ICD-10: Z36.0, O28.5 Clinical summary This test evaluates maternal serum levels of four specific markers to assess the risk of fetal chromosomal abnormalities and neural tube defects.
TEST-1176 Quantitative Fluorescence PCR (QF‑PCR) Panel for Chromosomes 13, 18, 21, and XY Test This diagnostic test rapidly evaluates amniotic fluid, chorionic villi, or cord blood for common aneuploidies involving chromosomes 13, 18, 21, and the XY sex chromosomes.	Amniotic Fluid, Chorionic Villi, or Cord Blood	1 – 2 Business Days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Presence of extra chromosomes 13, 18, 21", "Sex chromosome abnormalities (XY)"] Parameters [] Preparation ["No specific patient preparation required.", "Do not discontinue prescribed pregnancy medications without consulting the physician."] Indications ["High-risk pregnancies", "Advanced maternal age", "Abnormal prenatal screening results", "Family history of chromosomal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 82134-2 ICD-10: Z36.0 Clinical summary This diagnostic test rapidly evaluates amniotic fluid, chorionic villi, or cord blood for common aneuploidies involving chromosomes 13, 18, 21, and the XY sex chromosomes.
TEST-201 Quantitative Urine Amino Acids (Full Panel Test This test quantitatively measures 45 amino acids in urine to screen for and diagnose inborn errors of metabolism.	Urine (first-morning, midstream, sterile container)	3 working days (Mon/Wed by 5 PM)	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Quantitative levels of 45 amino acids", "Amino acid metabolism"] Parameters [{"name": "Alanine", "reference_range": null}, {"name": "Arginine", "reference_range": null}, {"name": "Asparagine", "reference_range": null}, {"name": "Aspartate", "reference_range": null}, {"name": "Cysteine", "reference_range": null}, {"name": "Glutamate", "reference_range": null}, {"name": "Glutamine", "reference_range": null}, {"name": "Glycine", "reference_range": null}, {"name": "Histidine", "reference_range": null}, {"name": "Isoleucine", "reference_range": null}, {"name": "Leucine", "reference_range": null}, {"name": "Lysine", "reference_range": null}, {"name": "Methionine", "reference_range": null}, {"name": "Phenylalanine", "reference_range": null}, {"name": "Proline", "reference_range": null}, {"name": "Serine", "reference_range": null}, {"name": "Threonine", "reference_range": null}, {"name": "Tryptophan", "reference_range": null}, {"name": "Tyrosine", "reference_range": null}, {"name": "Valine", "reference_range": null}] Preparation ["Collect first-morning urine midstream in a sterile container", "Refrigerate or freeze sample immediately", "Disclose all supplements, protein powders, and nutritional shakes on the drug history form", "Do not discontinue prescribed medication or medical diet without physician guidance"] Indications ["Suspected inborn errors of metabolism", "Monitoring treatment response", "Guiding dietary adjustments", "Investigating developmental delay or seizures"] Measurement technique Confirm with laboratory Codes LOINC: 35164-6 ICD-10: Z13.228, R82.6 Clinical summary This test quantitatively measures 45 amino acids in urine to screen for and diagnose inborn errors of metabolism.
TEST-4561 RAB27A Gene Griscelli Syndrome Type 2 Genetic Test This test evaluates the entire coding region of the RAB27A gene for pathogenic variants associated with Griscelli syndrome type 2.	Whole Blood (EDTA) or Buccal Swab (DNA FTA Card)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the RAB27A gene", "Deletion/duplication analysis of the RAB27A gene"] Parameters [] Preparation ["No special preparation is needed", "Fasting is not required"] Indications ["Suspected diagnosis of Griscelli syndrome type 2 based on clinical presentation", "Family history of Griscelli syndrome type 2", "Carrier screening in at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 92822-5 ICD-10: E70.330 Clinical summary This test evaluates the entire coding region of the RAB27A gene for pathogenic variants associated with Griscelli syndrome type 2.
TEST-5107 RAD51 Gene Mirror Movements Type 2 Genetic Test This test evaluates the RAD51 gene for pathogenic variants associated with congenital mirror movements type 2 (CMM2) using next-generation sequencing.	Whole blood, DNA, dried blood spot (FTA card)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RAD51 gene variants (SNVs, indels, CNVs)", "Pathogenic variants linked to CMM2"] Parameters [] Preparation ["No fasting required", "Provide complete clinical history and pedigree chart to phlebotomist"] Indications ["Diagnosis of congenital mirror movements type 2 (CMM2)", "Family history of CMM2"] Measurement technique Confirm with laboratory Codes LOINC: 81252-9 ICD-10: G25.82 Clinical summary This test evaluates the RAD51 gene for pathogenic variants associated with congenital mirror movements type 2 (CMM2) using next-generation sequencing.
TEST-4579 RAG1 Gene (Severe Combined Immunodeficiency, B‑cell Negative) Genetic Test This genetic test identifies pathogenic variants in the RAG1 gene associated with B-cell negative Severe Combined Immunodeficiency (SCID). It detects sequence variants, deletions,...	Whole Blood (EDTA), Extracted DNA (≥2 µg), or FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RAG1 gene sequence variants", "RAG1 gene deletions", "RAG1 gene copy number variations (CNV)"] Parameters [] Preparation ["Complete clinical history questionnaire", "Mandatory pre-test genetic counselling session", "Do NOT stop prescribed medications without physician advice"] Indications ["Clinical suspicion of SCID", "Known family history of RAG1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81263-8 ICD-10: D81.1 Clinical summary This genetic test identifies pathogenic variants in the RAG1 gene associated with B-cell negative Severe Combined Immunodeficiency (SCID). It detects sequence variants, deletions, and copy number variations.
TEST-5311 RAG2 Gene Combined Cellular and Humoral Immune Defects with Granulomas Genetic Test This test uses Next-Generation Sequencing to analyze the entire coding region of the RAG2 gene for pathogenic variants linked to combined immunodeficiency with granulomas.	Whole Blood (EDTA tube), Extracted DNA (min 1 µg), or One Drop of Blood on FTA Card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RAG2 gene sequence", "Pathogenic variants (SNVs, indels, copy number variants)"] Parameters [] Preparation ["Provide detailed clinical history", "Mandatory genetic counselling session", "Construct comprehensive pedigree chart"] Indications ["Suspected combined cellular and humoral immune deficiency", "Family screening for RAG2-related disorders", "Research applications"] Measurement technique Confirm with laboratory Codes LOINC: 48707-5 ICD-10: D81.32 Clinical summary This test uses Next-Generation Sequencing to analyze the entire coding region of the RAG2 gene for pathogenic variants linked to combined immunodeficiency with granulomas.
TEST-2845 RAPSN Gene Fetal Akinesia Deformation Sequence Genetic Test (NGS) This test evaluates the RAPSN gene for pathogenic variants associated with fetal akinesia deformation sequence and congenital myasthenic syndrome.	Venous whole blood (EDTA), extracted DNA, or dried blood spot (FTA card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the RAPSN gene", "Presence of disease-causing mutations"] Parameters [] Preparation ["Detailed clinical history required", "Pre-test genetic counselling session mandatory", "Pedigree chart of affected family members needed"] Indications ["Prenatal diagnosis of FADS", "Diagnosis of congenital myasthenic syndrome", "Family history of RAPSN-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 82919-7 ICD-10: G70.2 Clinical summary This test evaluates the RAPSN gene for pathogenic variants associated with fetal akinesia deformation sequence and congenital myasthenic syndrome.
TEST-4026 RASA1 Gene Genetic Test for Capillary Malformation-Arteriovenous Malformation This test evaluates the RASA1 gene for pathogenic variants associated with Capillary Malformation-Arteriovenous Malformation (CM-AVM) syndrome.	Whole blood (EDTA tube), extracted DNA, or FTA card blood spot	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RASA1 gene pathogenic variants", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["Detailed clinical history documentation", "Genetic counselling session", "Three-generation pedigree chart"] Indications ["Suspected Capillary Malformation-Arteriovenous Malformation (CM-AVM) syndrome", "Family history of CM-AVM", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 50398-7 ICD-10: Q27.3 Clinical summary This test evaluates the RASA1 gene for pathogenic variants associated with Capillary Malformation-Arteriovenous Malformation (CM-AVM) syndrome.
TEST-5482 RBPJ Gene Adams-Oliver Syndrome Type 3 Genetic Test This test identifies pathogenic variants in the RBPJ gene associated with Adams-Oliver syndrome type 3.	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in RBPJ gene", "Copy Number Variants (CNVs) in RBPJ gene"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Suspected Adams-Oliver syndrome type 3", "Unexplained scalp defects", "Limb anomalies", "Congenital heart disease"] Measurement technique Confirm with laboratory Codes LOINC: 81306-6 ICD-10: Q87.8 Clinical summary This test identifies pathogenic variants in the RBPJ gene associated with Adams-Oliver syndrome type 3.

Category overview

Biochemistry: overview

Seeking clarity about your body's essential functions is vital for long-term well-being. At DNA Labs UAE, our Biochemistry services utilize advanced automated analyzers to evaluate enzymes, proteins, and metabolites in your blood. Whether you need routine metabolic panels or specialized biochemical testing in the UAE, these tests provide critical data to guide your physician's medical plan. As a leading diagnostic lab in Dubai and the UAE, we guarantee strict confidentiality and rapid, accurate turnaround times. Take charge of your health today. Explore our biochemistry diagnostics below, schedule a convenient home sample collection, or contact our specialists to book your test.

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Biochemistry tests in Dubai & UAE

Biochemistry test prices

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